Items where Author is "Rosendahl, Jonas"

2015

Buch, Stephan and Stickel, Felix and Trépo, Eric and Way, Michael and Herrmann, Alexander and Nischalke, Hans Dieter and Brosch, Mario and Rosendahl, Jonas and Berg, Thomas and Ridinger, Monika and Rietschel, Marcella and McQuillin, Andrew and Frank, Josef and Kiefer, Falk and Schreiber, Stefan and Lieb, Wolfgang and Soyka, Michael and Semmo, Nasser and Aigner, Elmar and Datz, Christian and Schmelz, Renate and Brückner, Stefan and Zeissig, Sebastian and Stephan, Anna-Magdalena and Wodarz, Norbert and Devière, Jacques and Clumeck, Nicolas and Sarrazin, Christoph and Lammert, Frank and Gustot, Thierry and Deltenre, Pierre and Völzke, Henry and Lerch, Markus M. and Mayerle, Julia and Eyer, Florian and Schafmayer, Clemens and Cichon, Sven and Nöthen, Markus M. and Nothnagel, Michael and Ellinghaus, David and Huse, Klaus and Franke, Andre and Zopf, Steffen and Hellerbrand, Claus and Moreno, Christophe and Franchimont, Denis and Morgan, Marsha Y. and Hampe, Jochen. (2015) A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature Genetics, 47 (12). pp. 1443-1448.

2011

Steiner, Bernhard and Rosendahl, Jonas and Witt, Heiko and Teich, Niels and Keim, Volker and Schulz, Hans-Ulrich and Pfützer, Roland and Löhr, Matthias and Lühr, Matthias and Gress, Thomas M. and Nickel, Renate and Landt, Olfert and Koudova, Monika and Macek, Milan and Farre, Antoni and Casals, Teresa and Desax, Marie-Claire and Gallati, Sabina and Gomez-Lira, Macarena and Audrezet, Marie Pierre and Férec, Claude and des Georges, Marie and Claustres, Mireille and Truninger, Kaspar. (2011) Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens. Human mutation, Vol. 32, H. 8. pp. 912-920.